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Improved progression-free survival in irinotecan-treated metastatic colorectal cancer patients carrying the HNF1A coding variant p. I27L
High-throughput genetic screening of 51 pediatric cataract genes identifies causative mutations in inherited pediatric cataract in south eastern Australia
Exome array analysis identifies variants in SPOCD1 and BTN3A2 that affect risk for gastric cancer
Gender differences in the association of ENPP1 polymorphisms with type 2 diabetes in a Chinese population
Functional polymorphisms in PD-L1 gene are associated with the prognosis of patients with early stage non-small cell lung cancer
Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations
The RAD51C exonic splice-site mutations c. 404G> C and c. 404G> T are associated with familial breast and ovarian cancer
Replicative Analysis Of 30 Snps In Russian Patients With Alzheimer’s Disease
Damaging Missense De Novo Coding Mutations Contribute To Schizophrenia Risk
Association of polymorphism in the dopamine receptors and transporter genes with hyperprolactinemia in patients with schizophrenia